Automation Engineer - Building Automation Systems
Automation Engineer - Building Automation Systems
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$ 80000 - 110000
1 Vacancy
Job Description
The Automation Engineer Building Automation Systems is responsible for oversight of operational and troubleshooting support for the utilities Automation System with strict adherence to Standard Operating Procedures (SOPs) and cGMPs in a Pharmaceutical Manufacturing facility. Will provide plant engineering support for projects as it relates to the utility control system and demonstrate skills in design configuration integration implementation and qualification of automation control solutions with integration to OSIPi historian.
This individual will work closely with a crossfunctional team to meet the needs of the groups they support.
Role that this position reports to: Sr. Manager Reliability Engineering
Responsibilities:
Responsible for providing engineering expertise to support the design installation commissioning validation and operation of the automation systems.
Accountable for the Utility Automation Reliability Program:
Execute the maintenance strategy for new and modified equipment
Management of CMMS data integrity and of Reliability Centered Maintenance Improvements
Develop preventative maintenance procedures for automation systems ensuring maintenance programs are implemented
Continuous Improvement of maintenance PMs BOMs and Spare Parts
Review and lead equipment replacement as part of the life cycle improvement process and continuous improvement initiative planning.
Implements and monitors predictive maintenance of the system
Oversees reconditioning of the equipment to restore to likenew condition
Performs upgrades to improve safety operational performance and extend operational life
Collaborates with local and global partners to develop asset management plan that includes capital requestsProvides technical expertise for all phases associated with the automation system provides improvements based on supporting data technical knowledge engineering principles and current industry practices.
Ensure cGMP compliance of all automation systems to meet regulatory compliance:
Equipment is maintained at a level required to provide high reliability maximizing useful life
Review environmental monitoring and laboratory sample release test results
Manage deviations investigations (CAPAs and OOTs) with ontime closure
Safely resolve process problems improve efficiency reduce waste and maximize uptime production
Execute root cause analysis around equipment and operational events owning change controls investigations
Lead investigations as the subject matter expert providing technical expertise for all phases associated with the operation and troubleshooting of the automation systems
Responsible for the development and maintenance of the control drawings flow diagrams and Standard Operational documents.
Perform inspections for quality assurance on a periodic basis and initiate any procedures necessary to resolve problems
Responsible for inspections (GEMBAs/audits) for quality assurance on a periodic basis.
Responsible for change control activities the implementation of CAPA items quality investigations and determine/implement long lasting corrective actions and preventative measures.Responsible to ensure control system data integrity and user friendly navigation with alarm rationalization strategic implementation for efficiency in alarm response
Support all aspects of Johnson Controls Metasys for Validated Environments software configuration tools and Rockwell Automation Control Systems. Understands coordination and communication protocols between platforms such as Allen Bradley MODBUS BACNet etc.
Perform and document hardware/software modifications and system functional specification updates in Collaboration with Systems.
Demonstrate continuous improvement with respect to increasing job knowledge and proficiency related to biopharmaceutical industry engineering best practices and technologies as well as technical understanding/problem solving capability.
Complies with requirements from CSL Behrings Safety Program including Health and Safety mandates and OSHA requirements.
Completes any other duties/responsibilities assigned by senior management.
Qualifications:
Bachelors Degree in Electrical or Mechanical Engineering preferred or B.S. degree in an Engineering related field.
3 years of relevant automation/controls experience and a BS
2 years of relevant experience and a MS
Must possess basic knowledge of core principles in various engineering disciplines (fluid mechanics heat transfer thermodynamics etc.
Strong programming/design handson experience with Building Automation System (Johnson Controls Siemens Honeywell Rockwell or other) and SCADA systems is required.
Experience configuring troubleshooting and using Windows Operating Systems Networking virtualization and Databases for Control System Applications
Experience with data historians (like OSIPI) MSSQL and reporting tools are required.
Working knowledge of Control and Instrumentation for facility control systems. Basic knowledge of programmable logic controllers (PLCs) instrumentation (e.g. flow pressure temperature level) and controls is required.
Working knowledge of pharmaceutical process sanitary connections valves and supply loops.
Experience with Quality Management and Change Control Systems.
Knowledge of computerized maintenance management systems (CMMS).
Excellent problemsolving skills and the ability to work in collaborative and independent work situations and environments with minimal supervision.
Demonstrated ability to manage contractors while interfacing with multiple departments working with internal customers to manage projects.
Knowledge of manufacturing processes
Computer skills: MS Project and AutoCAD preferred
The expected base salary range for this position at hiring is $80000 $110000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed location as of the time of this posting. Individual base salary for a successful candidate is determined by qualifications skill level experience competencies and other relevant factors. In addition to base salary total compensation for this role may also include incentive compensation and equity.
Our Benefits
CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits from health care to financial protection so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family need help paying for emergency back up care or summer camp looking for mental health resources planning for your financial future or supporting your favorite charity with a matching contribution CSL has many benefits to help achieve your goals.
Please take the time to review our benefits site to see whats available to you as a CSL employee.
About CSL Behring
CSL Behring is a global leader in developing and delivering highquality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology hematology cardiovascular and metabolic respiratory and transplant therapeutic areas. Learn more about CSL Behring.
We want CSL to reflect the world around us
As a global organization with employees in 35 countries CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.
Do work that matters at CSL Behring!
Employment Type
Full-Time
